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Serious recall: Injury is possible or has been reported. Take action promptly.

Mckesson Medical-Surgical Inc. Corporate Office 2024-03-20 Health serious FDA
Health · FDA · Recall #FDA-D-0371-2024

Rocuronium Bromide Injection, Preservative Free, 10 mg / mL, Multiple-Dose Vial 10 mL, Rx… Recall

Issued March 20, 2024 · Mckesson Medical-Surgical Inc. Corporate Office

In March 2024, Mckesson Medical-Surgical Inc. Corporate Office recalled the Rocuronium Bromide Injection, Preservative Free, 10 mg / mL, Multiple-Dose Vial 10 mL, Rx…, a serious health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.

Compiled by Maya Ellison, RecallCheckr

What this means for you

cGMP Deviations: Products were stored outside the drug label specifications.

What you should do

  1. 1 Stop using Rocuronium Bromide Injection, Preservative Free, 10 mg / mL, Multiple-Dose Vial 10 mL, Rx… right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact Mckesson Medical-Surgical Inc. Corporate Office to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
Mckesson Medical-Surgical Inc. Corporate Office
Category
Health
Recall date
March 20, 2024
Units affected
Not reported
Sold at
Product was distributed to three direct accounts in NM, AZ and UT.
Recall number
FDA-D-0371-2024
Made in
United States
Issuing agency
FDA

In context

Read the official FDA notice

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